Half-sandwich ruthenium (II) compounds comprising nitrogen containing ligands for treatment of cancer

ABSTRACT

Ruthenium (II) compounds of the formula: 
                 
 
wherein: R 1  is —CO 2 CH 3 ; R 2 , R 3 , R 4 , R 5  and R 6  independently represent H, alkyl, cylcoalkyl, —CO 2 R′, aryl or alkylaryl, which latter two groups are optionally substituted on the aromatic ring; R′ represents alkyl, cylcoalkyl, aryl or alkaryl; X is halo, H 2 O, (R′)(R″)SO, R′CO 2   −  or (R′)(R″)C═O, where R″ represents alkyl, cylcoalkyl, aryl or alkaryl; Y is a counterion; m is 0 or 1; q is 1, 2 or 3; C′ is C 1  to C 12  alkylene, optionally substituted in or on the alkylene chain, bound to two A groups; p is 0 or 1 and r is 1 when p is 0 and r is 2 when p is 1; and A and B are: each independently R 11 —CN, where R″ represents alkyl or cycloalkyl; or B is halo and A is 4-substitued pyridine; or p is 0, A is NR 7 R 8  and B is NR 9 R 10 wherein R 7 , R 8 , R 9  and R 10  independently represent H, or alkyl, and A and B are linked by an alkylene chain, optionally substituted in or on the alkylene chain; or p is 1, A is NR 7  and B is NR 9 R 10 , wherein R 7 , R 9  and R 10  are as previously defined, and A and B are linked by an alkylene chain, optionally substituted are described.

This application is a continuation of U.S. application Ser. No. 10/134,404, filed Apr. 26, 2002, now U.S. Pat. No. 6,750,251, which is a continuation of PCT/GB00/04144, filed Oct, 26, 2000, which claims priority to GB application no. 0016054.9, filed Jun. 30, 2000 and GB application no. 9925274.4, filed Oct. 27, 1999, both of which are hereby incorporated by reference.

This invention relates to ruthenium (II) compounds, to their use in medicine, particularly for the treatment and/or prevention of cancer, and to a process for their preparation.

Certain ruthenium (II) complexes have been proposed for use in treating cancer. For example, U.S. Pat. No. 4,980,473 discloses 1,10-phenanthroline complexes of ruthenium (II) and cobalt (III) which are said to be useful for the treatment of tumour cells in a subject.

Some other ruthenium (II) and ruthenium (III) complexes which have been shown to exhibit antitumour activity are mentioned in Guo et al, Inorganica Chimica Acta, 273 (1998), 1-7, specifically trans-[RuCl₂(DMSO)₄], trans-[RuCl₂(imidazole)₂]- and trans-[RuCl₄(indazole)₂]⁻. Guo et al discloses that the most interesting feature of these complexes is their anti-metastatic activity. Clarke et al have reviewed the anticancer and in particular the antimetastatic activity of ruthenium complexes: Chem. Rev. 1999, 99, 2511-2533. Also, Sava has reveiwed the antimetastatic activity in “Metal Compounds in Cancer Therapy” Ed by S P Fricker, Chapman and Hall, London 1994, p. 65-91.

Dale et al, Anti-Cancer Drug Design (1992), 7, 3-14, describes a metronidazole complex of ruthenium (II) ie, [(η⁶-C₆H₆)RuCl₂(metronidazole)] and its effect on DNA and on E. coli growth rates. Metronidazole sensitises hypoxic tumour cells to radiation and appears to be an essential element of the complexes of Dale et al. There is no indication in Dale et al that the complexes would be at all effective in the absence of the metronidazole ligand.

Krämer et al, Chem Eur J., 1996, 2, No. 12, p. 1518-1526 discloses half sandwich complexes of ruthenium with amino esters.

There exists a need for novel anticancer compounds which can be used as alternatives to the compounds which are currently available.

The present invention provides a novel class of ruthenium (II) complexes having anti-tumour activity.

According to the present invention there is provided a ruthenium (II) compound of formula (I):

wherein: R¹, R², R³, R⁴, R⁵ and R⁶ independently represent H, alkyl, —CO₂R′, aryl or alkylaryl, which latter two groups are optionally substituted on the aromatic ring;

R′ represents alkyl, aryl or alkaryl;

X is halo, H₂O, (R′)(R″)SO, R′CO₂ ⁻ or (R′)(R″)C═O, where R″ represents alkyl, aryl or alkaryl;

Y is a counterion;

m is 0 or 1;

q is 1, 2 or 3;

C′ is C₁ to C₁₂ alkylene, optionally substituted in or on the alkylene chain, bound to two A groups;

p is 0 or 1 and r is 1 when p is 0 and r is 2 when p is 1; and

A and B are: each independently N-donor nitrile ligands; or B is halo and A is an N-donor pyridine ligand, optionally substituted at one or more of the carbon atoms of the pyridine ring; or p is 0, A is NR⁷R⁸ and B is NR⁹R¹⁰, wherein R⁷, R⁸, R⁹ and R¹⁰ independently represent H or alkyl, and A and B are linked by an alkylene chain, optionally substituted in or on the alkylene chain; or p is 1, A is NR⁷ and B is NR⁹R¹⁰, wherein R⁷, R⁹ and R¹⁰ are as previously defined, and A and B are linked by an alkylene chain, optionally substituted.

The compounds of the invention may be in the form of solvates and/or prodrugs. Prodrugs are variants of the compounds of the invention which can be converted to compounds of formula (I) in vivo.

The compounds of formula (I) may have one or more chiral centres. When the compounds of formula (I) have one or more chiral centres, they may be in the form of one enantiomer, may be enriched in one enantiomer or may be a racemic mixture.

The term “alkyl” as used herein includes C₁ to C₆ allyl groups which may be branched or unbranched. Unbranched alkyl groups include, for example, methyl, ethyl, propyl, butyl, pentyl and hexyl. Branched alkyl groups include, for example, 2-propyl, 2-butyl and 2-(2-methyl)propyl. The alkyl groups in the compounds of the invention may optionally be substituted. Substituents include one or more further alkyl groups and/or one or more further substituents, such as, for example, cyano, nitro, hydroxyl, haloalkyl, —CO₂alkyl, halo, thiol (SH), thioether (eg, S-alkyl) and sulfonate. The term “alkylene” is defined similarly to the definition of the term “alkyl” bu includes C₂ to C₁₂ groups and is a divalent species with radicals separated by two or more (eg, from two to twelve) carbon atoms linked in a chain. Preferably, the alkylene groups are straight chain groups. Alkylene groups are optionally substituted in the alkylene chain, preferably with one or more phenylene (eg, 1,4-phenylene) and/or —CONR^(1a)-groups and/or —NR^(2a)-groups, where R^(1a) and R^(2a) independently represent H, alkyl, aryl or alkaryl. Preferably, R^(1a) and R^(2a) are H or C₁ to C₃ alkyl.

Cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.

The term “aryl” as used herein includes aromatic carbocyclic rings such as phenyl and naphthyl and heterocyclic rings such as pyridyl, imidazolyl, pyrrolyl and furanyl. Aryl groups may optionally be substituted with one or more substituents including, for example, alkyl, cyano, nitro, hydroxyl, haloalkyl, —CO₂alkyl, halo, thiol (SH), thioether (eg, S-alkyl) and sulfonate.

The term “alkaryl” means alkyl substituted with aryl eg, benzyl.

The term “halo” means a halogen radical selected from fluoro, chloro, bromo and iodo.

The term “haloalkyl” means alkyl substituted with one or more halo groups eg, trifluoromethyl.

In the compounds of formula (I), R¹, R², R³, R⁴, R⁵ and R⁶ may represent H. Alternatively, R¹ may be 2-propyl and R⁴ may be methyl, with R², R³, R⁵ and R⁶ all representing hydrogen. As a further alternative, R¹ may be phenyl, with R², R³, R⁴, R⁵ and R⁶ all representing hydrogen. In a yet further alternative, R¹ may be —CO₂R′, such as —CO₂CH₃ for example, with R², R³, R⁴, R⁵ and R⁶ all representing hydrogen.

In one aspect, A and B in the compounds of formula (I) both represent R¹¹—CN. R¹¹ is alkyl, preferably C₁ to C₃ alkyl, more preferably methyl.

In another aspect, one of A and B in the compounds of formula (I) represents a 4-substituted pyridine and the other represents halo. The pyridine may be substituted at the 4-position by, for example, groups including nitro, cyano and C(O)NR¹²R¹³ wherein R¹² and R¹³ are independently selected from H and alkyl (eg, C₁ to C₆ alkyl). The group at the 4-position of the pyridine ring is preferably an electron withdrawing group.

In a further aspect, A and B may together represent NR⁷R⁸—(CR¹²R¹³)_(n)—NR⁹R¹⁰, wherein R¹² and R¹³ are independently H or alkyl or R¹² and R¹³ groups, on the same carbon atom or on neighbouring carbon atoms, are linked to form a carbocylic ring and n is an integer from 1 to 4. Preferably, R¹² and R¹³ are both hydrogen and n is 2 or 3, more preferably 2. R⁷, R⁸, R⁹ and R¹⁰ are preferably H or methyl and, more preferably, all of R⁷, R⁸, R⁹ and R¹⁰ are H.

When R⁸ is present in A, then p is 0. When R⁸ is absent, then p is 1.

In a further aspect of the invention, R⁸ is absent from A, p is 1 and C′ is C₄ to C₁₀ straight chain alkylene (eg, hexylene). Compounds according to this aspect of the invention are so-called dinuclear complexes comprising two ruthenium atoms per complex.

Other examples of dinuclear complexes of the invention are those in which A and B together represent:

wherein each n′, n″, x′, x″ and y′ independently represents an integer from 1 to 12, preferably 1 to 6.

Y^(q−) in compounds of formula (I) is a counterion and is only present in the compound when the complex containing the metal ion is charged. Y^(q−) is preferably a non-nucleophilic anion such as PF₆ ⁻, for example.

R′ and R″ are preferably alkyl. Most preferably, both R′ and R″ are methyl.

Compounds of formula (I) may be used in medicine. In particular, compounds of formula (I) may be used to treat and/or prevent cancer.

Therefore, the present invention also provides the use of a compound of the invention (ie, a compound of formula (I)) in the manufacture of a medicament for the treatment and/or prevention of cancer.

Further provided by the invention is a method of treating and/or preventing cancer which comprises administering to a subject a therapeutically effective amount of a compound of the invention.

The compounds of the invention may be used directly against a tumour. Alternatively or additionally, the compounds may be used to prevent or inhibit metastasis and/or to kill secondary tumours. It will be understood that the prevention or inhibition of metastasis is encompassed by the term “preventing cancer”, as used herein.

The invention also provides a pharmaceutical composition comprising one or more compounds of the invention together with one or more pharmaceutically acceptable excipients. Suitable excipients include diluents and/or carriers.

The compounds of the invention may be administered by a number of routes including, for example, orally, parenterally (eg, intramuscularly, intravenously or subcutaneously), topically, nasally or via slow releasing microcarriers. Thus, suitable excipients for use in the pharmaceutical compositions of the invention include saline, sterile water, creams, ointments, solutions, gels, pastes, emulsions, lotions, oils, solid carriers and aerosols.

The compositions of the invention may be formulated in unit or sub-unit dosage form including, for example, tablets, capsules and lozenges and containers containing the composition in a form suitable for parenteral administration.

The specific dosage level of the compounds and compositions of the invention will depend upon a number of factors, including the biological activity of the specific compound used and the age, body weight and sex of the subject. It will be appreciated that the subject may be a human or a mammalian animal.

The compounds and compositions of the invention can be administered alone or in combination with other compounds. The other compounds may have a biological activity which complements the activity of the compounds of the invention eg, by enhancing its effect in killing tumours or by reducing any side-effects associated with the compounds of the invention.

The present invention also provides a process for preparing the compounds of the invention which comprises the reaction of a compound of formula [(η⁶-C₆(R¹)(R²)(R³)(R⁴)(R⁵)(R⁶))RuX₂], which may be in the form of a monomer or a dimer, with A and B, optionally in the presence of Y^(q−), in a suitable solvent for the reaction, wherein R¹, R², R³, R⁴, R⁵, R⁶, X, A, B and Y are as defined above for the compounds of the invention.

Suitable compounds of formula [(η⁶-C₆(R¹)(R²)(R³)(R⁴)(R⁵)(R⁶))RuX₂] for use as starting materials (starting ruthenium complexes) in the process of the invention include [(η⁶-C₆H₆)RuCl₂]₂, [(η⁶-C₆H₆)RuBr₂]₂, [(η⁶-C₆H₆)RuI₂]₂, [(η⁶-p-cymene)RuCl₂]₂, [(η⁶-p-cymene)RuBr₂]₂ and [(η⁶-p-cymene)RuI₂]₂ which can be prepared by known methods eg Bennett et al, J. Chem. Soc. Dalton Trans., 1974, 233.

When A and B in the compounds of the invention are R¹¹—CN, the solvent for the reaction may be R¹¹—CN itself. Preferred reaction conditions include stirring the starting ruthenium complex, as described above, in R¹¹—CN as solvent at room temperature until a sufficient amount of product is formed. The reaction mixture comprises a source of Y^(q−), such as a compound of formula (NH₄ ⁺)Y^(q−) eg, NH₄PF₆.

Compounds of formula (I) in which A and B represent, together, NR⁷R⁸—(CR¹²R¹³)_(n)—NR⁹R¹⁰ or NR⁹R¹⁰—(CR¹²R¹³)_(n)—NR⁷—C′—NR⁷—(CR¹²R¹³)_(n)—NR⁹R¹⁰ can be produced, according to the process of the invention, by stirring the starting ruthenium complex in the presence of a slight excess of NR⁷R⁸—(CR¹²R¹³)_(n)—NR⁹NR¹⁰ or an equimolar amount of NR⁹R¹⁰—(CR¹²R¹³)_(n)—NR⁷—C′—NR⁷—(CR¹²R¹³)_(n)—NR⁹R¹⁰, respectively, in a suitable solvent, preferably an alcoholic solvent such as methanol. The reaction may be carried out at room temperature or at elevated temperature (eg, 30° C. to 90° C.) until a sufficient amount of product is formed; optionally after cooling the reaction mixture. The reaction mixture comprises a source of Y^(q−), such as a compound of formula (NH₄ ⁺)Y^(q−) eg, NH₄PF₆.

Compounds of formula (I) in which A or B is an N-donor pyridine ligand may be obtained, according to the process of the invention, by heating a mixture of the starting ruthenium complex and excess pyridine compound (such as a 1.5- to 3-fold molar excess) in a suitable solvent such as benzene until a sufficient amount of product is formed. The reaction may be carried out under reflux conditions.

The precipitate which is formed in the process of the invention comprises or consists of the compound of the invention. The compound of the invention may be isolated from the reaction mixture by separating the precipitate from the liquid phase (eg, by filtration) and then removing the solvent from the precipitate (eg, under reduced pressure). The solid thus formed, which comprises or consists of the compound of the invention may, optionally, be purified eg, by recrystallisation from a suitable solvent (including, for certain compounds of the invention, acetonitrile or acetonitrile/ether (where A and B are R¹¹—CN and R¹¹ is methyl) and methanol/ether).

The following non-limiting examples illustrate the present invention.

EXAMPLES A. Synthesis

General

The starting materials, [(η⁶-C₆H₆)RuCl₂]₂, [(η⁶-C₆H₆)RuBr₂]₂, [η⁶-C₆H₆)RuI₂]₂, [(η⁶-p-cymene)RuCl₂]₂, [(η⁶-p-cymene)RuBr₂]₂, [(η⁶-p-cymene)RuI₂]₂ were prepared as previously reported^(i). Acetonitrile was dried over CaH₂ and ethylenediamine distilled over Na metal prior to use.

The preparations of Examples 1 and 2 were based on a published synthesis^(ii) and followed the same general procedure.

Example 1 Preparation of [(η⁶-p-cymene)RuCl(CH₃CN)₂]⁺[PF₆]⁻

[(η⁶-p-cymene)RuCl₂]₂ (0.31 g, 0.51 mmol) was stirred in 20 ml reagent grade acetonitrile. NH₄PF₆ (0.18 g, 1.10 mmol) in 5 ml acetonitrile was added in one portion, the flask sealed without specific precautions to exclude air and the reaction stirred at room temperature. After 14 h the pale precipitate was filtered off and the orange filtrate evaporated to leave an orange solid. This was dissolved in the minimum hot acetonitrile, filtered and allowed to cool. Ether was added until precipitation was obvious and the mixture placed in the freezer for 2 d. The precipitate was filtered, washed with ether and dried in vacuo.

Yield: 0.28 g, 0.56 mmol, 54.9% C₁₄H₂₉ClF₆N₂PRu Calc. % C = 33.78 % H = 4.05 % N = 5.62 (497.82) Found % C = 33.80 % H = 3.91 % N = 5.53

Example 2 Preparation of [(η⁶-p-cymene)RuBr(CH₃CN)₂]⁺[PF₆]⁻

Procedure as in Example 1. [(η⁶-p-cymene)RuBr₂] (0.24 g, 0.3 mmol), NH₄PF₆ (0.12 g, 0.74 mmol), dry acetonitrile (12 ml). Final product recrystallised from acetonitrile/ether as deep red crystals.

Yield: 0.28 g, 0.52 mmol, 86.67% C₁₄H₂₀BrF₆N₂PRu Calc. % C = 31.01 % H = 3.72 % N = 5.16 (542.27) Found % C = 31.22 % H = 3.75 % N = 5.09

The ethylenediamine complexes of Examples 3 to 6 were prepared in the following manner^(i):

Example 3 Preparation of [(η⁶-C₆H₆)RuCl(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

[(η⁶-C₆H₆)RuCl₂]₂ (0.167 g, 0.33 mmol) was suspended in dry methanol (50 ml) and ethylenediamine (0.06 g, 1 mmol) added in one portion. This was stirred for 3 h, filtered and NH₄PF₆ (0.5 g, 3.07 mmol) added. The volume was slowly reduced to approx. 15 ml on the rotary evaporator. The product formed as a microcrystalline solid on leaving to stand at 4° C. This was collected, washed with ether and recrystallised from methanol/ether.

Yield: 0.128 g, 0.31 mmol, 46.96% C₈H₁₄ClF₆N₂PRu Calc. % C = 22.89 % H = 3.36 % N = 6.67 (419.69) Found % C = 22.81 % H = 3.24 % N = 6.51

Example 4 Preparation of [(η⁶-C₆H₆)RuI(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

Procedure as in Example 3. [(η⁶-C₆H₆)RuI₂]₂ (0.48 g, 0.55 mmol), dry methanol (80 ml), ethylenediamine (0.12 g, 2 mmol), NH₄PF₆ (0.5 g, 3.07 mmol).

Yield: 0.412 g, 0.81 mmol, 73.27% C₈H₁₄IF₆N₂PRu Calc. % C = 18.80 % H = 2.76 % N = 5.48 (511.14) Found % C = 18.52 % H = 2.43 % N = 5.14

Example 5 Preparation of [(η⁶-p-cymene)RuCl(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

Procedure as in Example 3. [(η⁶-p-cymene)RuCl₂] (0.39 g, 0.64 mmol), methanol (60 ml), ethylenediamine (0.12 g, 2.00 mmol). The reaction was stirred for 1.5 h and the green liquid filtered. NH₄PF₆ (0.52 g, 3.2 mmol) was added to the yellow filtrate and the volume reduced to 15 ml. This was left to stand at 4° C. for 6 h during which time orange crystals formed.

Yield 0.23 g, 0.48 mmol, 37.73% C₁₂H₂₂ClF₆N₂PRu Calc. % C = 30.29 % H = 4.66 % N = 5.88 (475.81) Found % C = 30.05 % H = 4.41 % N = 5.98

Example 6 Preparation of [(η⁶-p-cymene)RuI(H₂NCH₂CH₂NH₂—N, N)]⁺[PF₆]⁻

Procedure as in Example 3. [(η⁶-p-cymene)RuI₂] (0.34 g, 0.348 mmol), ethylenediamine (0.06 g, 1 mmol), NH₄PF₆ (0.52 g, 3.2 mmol). The volume was reduced to 15 ml and left stand at 4° C. overnight during which red crystals formed.

Yield: 0.235 g, 0.41 mmol, 59.48% C₁₂H₂₂IF₆N₂PRu Calc. % C = 25.41 % H = 3.91 % N = 4.94 (567.26) Found % C = 25.64 % H = 3.72 % N = 5.24

Example 7 Preparation of [(η⁶-p-cymene)RuCl₂(isonicotinamide)]

[(η⁶-p-cymene)RuCl₂] (0.129 g, 0.21 mmol) was set stirring in benzene (50 ml) and isonicotinamide (0.052 g, 0.43 mmol) added in one portion. The mixture was heated to reflux under argon for 4 h during which time a mustard coloured precipitate had formed. This was collected, washed with a little benzene and recrystallised from methanol/ether to give a red crystalline material.

Yield: 0.061 g, 0.142 mmol, 33.81% C₁₆H₂₀Cl₂N₂ORu Calc. % C = 44.87 % H = 4.71 % N = 6.54 (428.30) Found % C = 44.65 % H = 4.54 % N = 6.23

Example 8 Preparation of [η⁶-C₆H₅CO₂CH₃)RuCl(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

(a) Preparation of 1,4-dihydrobenzoic acid^(iv)

Benzoic acid (15.5 g, 0.13 mmol) was added to dry ethanol (100 ml) in a 1 l flask equipped with a mechanical stirrer, Dewar condenser and cooling bath (dry ice/acetone). NH₃ (600 ml) was condensed into the flask and Na metal (8.3 g, 0.36 mmol) added in small pieces over a period of 30 min. When the final blue colour was discharged the mixture was left to stir for 20 min after which time solid NH₄Cl (20 g, 0.22 mol) was carefully added. The cooling bath was removed and the NH₃ allowed to evaporate with stirring, leaving a white residue. The residue was taken up in chilled H₂O (500 ml) and acidified to about pH3 by addition of 10% HCl. This was extracted with ether (4×200 ml) and the combined ether layers washed with saturated NaCl solution (1×100 ml) and dried over MgSO₄. The ether was removed on the rotary evaporator leaving a crude oil which was distilled under reduced pressure giving a clear oil.

Yield: 13.56 g, 109 mmol, 90.8%

(b) Preparation of 3-methoxycarbonylcyclohexa-1,4-diene

Concentrated H₂SO₄ (1 ml) was added to a solution of 1,4-dihydrobenzoic acid (3 g, 23.97 mmol) in freshly dried methanol (10 ml). The reaction was heated to reflux in air for 1 h, cooled, poured into H₂O (25 ml) and extracted with ether (3×50 ml). The combined ether layers were washed with 5% Na[HCO₃] solution (50 ml) and saturated NaCl solution (50 ml) and dried over MgSO₄. The ether was removed on the rotary evaporator to leave a colourless oil which was used without further purification.

Yield: 2.60 g, 18.80 mmol, 42.8%

(c) Preparation of [(η⁶-C₆H₅CO₂CH₃)RuCl₂]₂

3-methoxycarbonylcyclohexa-1,4-diene (2.6 g, 18.80 mmol) was added to a filtered solution of RuCl₃.3H₂O (1 g, 3.80 mmol) in methanol (50 ml). The reaction was heated to reflux for 8 h under argon. The reaction was cooled, filtered and the volume reduced to 20 ml. After standing for 12 h at 4° C. the precipitate was collected, washed with a little methanol followed by ether and dried in vacuo.

Yield = 1.08 g, 1.75 mmol, 93.1% C₁₆H₁₆Cl₄O₄Ru₂ (616.24) Calc. % C = 31.18 % H = 2.62 Found % C = 31.05 % H = 2.39 (d) Preparation of [(η⁶-C₆H₅CO₂CH₃)RuCl(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

Ethylenediamine (0.09 g, 1.5 mmol) was added to a stirring suspension of [(η⁶-C₆H₅CO₂CH₃)RuCl₂]₂ (0.355 g, 0.576 mmol) in methanol (200 ml). After 4 h the orange solution was filtered and the volume reduced to 20 ml. NH₄PF₆ (0.49 g, 2.3 mmol) was added and the mixture stirred for a further minute. The sealed flask was left to stand overnight at 4° C. The precipitated yellow microcrystalline solid was collected, washed with a little methanol followed by ether and dried in vacuo.

Yield 0.22 g, 0.46 mmol, 40.0% C₁₀H₁₆ClN₂O₂PF₆Ru Calc. % C = 25.14 % H = 3.38 % N = (477.75) 5.86 Found % C = 25.18 % H = 3.12 % N = 5.50

Example 9 Preparation of [(η⁶-C₆H₅C₆H₅)RuCl(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

(a) Preparation of 1,4-dihydrobiphenyl^(v)

A solution of biphenyl (10 g, 65 mmol) in freshly dried THF (200 ml) was added to NH₃ (400 ml) which had been condensed under argon into a 1 l flask equipped with a Dewar condenser, cooling bath (dry-ice/acetone) and mechanical stirrer. Li wire (1.125 g, 162 mmol) was added in small pieces over a period of 15 min. After a further 15 min stirring, solid NH₄Cl (15 g, 280 mmol) was added and the dark red colour discharged.

The reaction was stirred at −60° C. for 10 min, then the cooling bath removed and the NH₃ allowed to evaporate under argon flow with stirring. The remaining residue was taken up in H₂O (200 ml) and acidified to pH3 with 10% HCl. This was extracted with ether (4×150 ml), and the combined ether layers washed with saturated NaCl solution (1×150 ml) and dried over MgSO₄. The ether was removed on the rotary evaporator and the remaining oil distilled under reduced pressure (46° C., 0.2 mmHg) to give clear oil which was used without further purification.

Yield: 6.45 g, 41.26 mmol, 63.5%

(b) Preparation of [(η⁶-C₆H₅C₆H₅)RuCl₂]₂

RuCl₃.3H₂O (2.28 g, 8.7 mmol) was dissolved in dry ethanol (25 ml) and filtered. 1,4-Dihydrobiphenyl (2.43 g, 15.5 mmol) was added in one portion and the solution heated to reflux under argon for 4 h. On cooling a brown solid settled out of solution. This was collected, washed with a little ethanol followed by ether and dried in vacuo.

Yield: 2.77 g, 8.49 mmol, 97.6% C₂₄H₂₄Cl₄Ru₂ (652.36) Calc. % C = 44.19 % H = 3.71 Found % C = 44.67 % H = 3.25 (c) Preparation of [(η⁶-C₆H₅C₆H₅)RuCl(H₂NCH₂CH₂NH₂—N,N)]⁺[PF₆]⁻

[(η⁶-C₆H₅C₆H₅)RuCl₂]₂ (0.30 g, 0.46 mmol) was refluxed in H₂O (25 ml) for 1 h. At this time ethylenediamine (0.06 g, 1 mmol) was added to the refluxing suspension. The brown suspension immediately became, dark green. This was refluxed for a further 30 min and filtered while hot. NH₄PF₆ (0.5 g, 3 mmol) was added to the yellowish filtrate and the flask briefly shaken. A yellow precipitate began to form almost immediately. The flask was sealed, allowed to cool to ambient temperature and placed in an ice-bath for 3 h. The precipitate was collected, washed with a little water, followed by ethanol, followed by ether and dried in vacuo. This was recrystallised from methanol/ether.

Yield: 0.11 g, 0.22 mmol, 23.9% C₁₄H₁₈ClF₆N₂PRu Calc. % C = 33.91 % H = 3.66 % N = 5.65 (495.82) Found % C = 34.06 % H = 3.37 % N = 5.44

Example 10 Preparation of {(η⁶-C₆H₅C₆H₅)RuCl[H₂N(CH₂)₂NH(CH₂CH₃)]}⁺PF₆ ⁻

[(η⁶-C₆H₅C₆H₅)RuCl₂]₂ (0.10 g, 0.158 mmol) was refluxed in water (10 ml) for 3 h and then cooled down to 80° C. To this suspension was added N-ethylethylenediamine (37 mg, 0.42 mmol) The brown suspension immediately became dark green. This was then slowly heated to reflux again for a further 1.5 h and filtered while hot. NH₄PF₆ (0.2 g, 1.23 mmol) was added to the yellowish filtrate and the flask briefly shaken. A yellow precipitate began to form almost immediately. After standing at 4° C. overnight, the precipitate was collected, washed with a little methanol followed by diethyl ether and dried in vacuo. This was recrystallised from methanol/ether.

Yield: 0.08 g, 0.153 mmol, 48.3% C₁₆H₂₂ClF₆N₂PRu Calc. % C = 36.68 % H = 4.23 % N = 5.35 (523.85) Found % C = 36.00 % H = 4.37 % N = 5.24

Example 11 Preparation of {[η⁶-C₆H₅C₆H₅)RuCl]₂[H₂N(CH₂)₂NH(CH₂)₆NH(CH₂ ₂NH₂—N,N′,N″,N′″]}²⁺2PF₆ ⁻

The starting material [(η⁶-C₆H₅C₆H₅)RuCl₂]₂ was prepared as previously described. Ethylenediamine and triethylamine were freshly distilled over Na. Tetrahydrofuran (THF) was dried by distillation from Na-benzophenone. Triphenylmethyl chloride (99%) and adipoyl chloride (98%) were purchased from the Arcos Chemical Co. All other chemicals were AR grade and were used as received.

(a) N-tritylethyldiamine

A solution of trityl chloride (5.57 g, 20 mmol) in dichloromethane (25 ml) was slowly added into a solution of ethylenediamine (8 ml, 120 mmol) in dichloromethane (75 ml) with stirring at room temperature. The addition was accomplished within 1 h and the reaction stirred overnight. The white salt was filtered off and the filtrate washed with water and dried over anhydrous sodium sulphate. Dichloromethane was removed by rotary evaporation and the residue dissolved into methanol. A white precipitate began to form after shaking for a while and the mixture was kept in the refrigerator for 5 h and then filtered off. The methanol filtrate was reduced to 10 ml and kept in the refrigerator overnight. A white solid precipitated. This was collected as the desired product and washed with diethyl ether and dried in vacuo.

Yield: 4.5 g, 14.88 mmol, 74.4%,

(b) N,N′-Bis(2′tritylaminoethyl)-1,6-diamidohexane

N-Tritylethyldiamine (1.5 g, 4.96 mmol) and triethylamine (1.0 g, 7.29 mmol) were dissolved in chloroform (35 ml) and cooled in an ice bath. To this solution was added adipoyl chloride (0.36 ml, 2.48 mmol) in chloroform (10 ml) slowly with stirring. After addition, the mixture was refluxed for 2 h and cooled to room temperature. This was filtered to give a clear chloroform filtrate (see below). The filtered precipitate was dissolved into dichloromethane. This was washed with water and then saturated NaCl solution and dried over anhydrous sodium sulphate. Removal of the solvent by rotary evaporation gave a white product. The chloroform filtrate was also washed with water and saturated NaCl solution and dried over anhydrous sodium sulphate. After removal of chloroform, a further crop of product was obtained.

Yield: 1.40 g, 1.91 mmol, 77% C₄₈H₅O₂N₄H₂O Calc. % C = 78.66 % H = 7.15 % N = 7.64 (732.96) Found % C = 78.81 % H = 6.73 % N = 7.55 (c) N,N′-Bis(2′-tritylaminoethyl)-1,6-diaminohexane

Into a solution of N,N′-bis(2′-tritylamninoethyl)-1,6-diamidohexane (1.3 g, 1.82 mmol) in dry THF was added a suspension of LiAlH₄ (0.69 g, 18.18 mmol) in dry THF (20 ml) under argon with vigorous stirring. After the addition, the reaction was heated to a gentle reflux with stirring for 25 h. This was cooled to 4° C. The reaction product and excess of hydride were decomposed by the dropwise addition of H₂O (0.69 ml), followed by 15% (w/v) NaOH solution (0.69 ml) and H₂O (2.07 ml) in succession. After vigorous stirring for 30 min. the mixture was filtered by suction and the resulting cake was washed thoroughly with dichloromethane. The combined filtrate was concentrated to dryness on the rotary evaporator and the resulting residue dissolved into dichloromethane (50 ml). This was washed with water and then saturated NaCl solution and dried over anhydrous sodium sulphate. Removal of dichloromethane by rotary evaporator afforded a colourless solid.

Yield: 1.20 g, 1.75 mmol, 96%

(d) N,N′-Bis(2-aminoethyl)-1,6-diaminohexane tetrahydrochloride

A mixture of N,N′-bis(2′-tritylaminoethyl)-1,6-diaminohexane (1.0 g. 1.45 mmol) and 6 M HCl (30 ml) was refluxed for 3 h. Then the mixture was filtered and the filtrate was concentrated to about 3 ml over vacuo. Addition of methanol into the concentrated solution afforded a white salt.

Yield: 0.46 g, 1.32 mmol, 92% C₁₀H₂₆N₄.4HCl Calc. % C = 34.48 % H = 8.68 % N = 16.09 (348.09) Found % C = 34.26 % H = 8.77 % N = 16.24 (e) {[η⁶-C₆H₅C₆H₅)RuCl]₂[H₂N(CH₂)₂NH(CH₂)₆NH(CH)₂NH₂—N,N′,N″,N′″]}²⁺2PF₆ ⁻

[(η⁶-C₆H₅C₆H₅)RuCl₂]₂ (0.106 g, 0.162 mmol) in 10 ml water was refluxed for 2.5 h and then cooled to 50° C. Into this suspension was added a solution of N,N′-bis(2-aminoethyl)-1,6-diaminohexane (0.162 mml) in methanol which was obtained by the treatment of N,N′-bis(2′-aminoethyl)-1,6-diaminohexane tetrahydrochloride (56.39 g, 0.162 mmol) with 1.294 ml 0.5008 N KOH-MeOH solution. The mixture was then heated to reflux for 1.5 h. This was filtered while hot. NH₄PF₆ (0.175 g, 1.07 mmol) was added into the bright yellow filtrate to yield a bright yellow precipitate. This was recrystallized from methanol/ether.

Yield: 0.10 g, 0.093 mmol, 57.5% C₃₄H₄₆Cl₂F₁₂N₄P₂Ru₂ Calc. % C = 38.03 % H = 4.32 % N = (1073.74) 5.22 Found % C = 37.86 % H = 4.25 % N = 5.20 B. Biological Data 1. Protocol for Testing Ru Compounds

The compounds are tested on 24-well trays. Cells growing in a flask are harvested just before they become confluent, counted using a haemocytometer and diluted down with media to a concentration of 1×10⁴ cells per ml. The cells are then seeded in the 24-well trays at a density of 1×10⁴ cells per well (i.e. 1 ml of the diluted cell suspension is added to each well). The cells are then left to plate down and grow for 72 hours before adding the compounds of the invention.

The Ru complexes are weighed out and made up to a concentration of 1 mg/ml with deionised water then sonicated until they go into solution. The appropriate volume of the Ru solution is added to 5 ml of media to make it up to a concentration of 100 μM for each drug. This 100 μM solution is then serially diluted to make up the 10 μM, 1 μM and 0.1 μM solutions.

The media is removed from the cells and replaced with 1 ml of the media dosed with drug. Each concentration is done in duplicate. A set of control wells are left on each plate, containing media without drug.

The cells are left exposed to the drugs for 24 hours and then washed with phosphate buffered saline before fresh media is added.

They are allowed to grow on for a further 3 days before being counted using a Coulter counter.

Preparing cells for counting:

Media is removed and 1 ml of PBS is added to the cells.

250 μl of trypsin is added and cells left in incubator for a few minutes to allow the monolayers to detach.

Once trypsinised, 250 μl of media is added to each well to neutralise the trypsin. 200 μl of this suspension is added to 10 ml of NaCl for counting.

2. Results

Using the above protocol, a number of compounds of the invention were tested on A2780 ovarian cancer cell line. The results are as follows:

Compound (Example No.) IC50 (μM) 1 7 2 8 7 11 5 8 4 20 3 8 6 6 9 6 8 55 10 6 11 5

References

-   (i) M. A. Bennett, A. K. Smith J. Chem. Soc. Dalton Trans. 1974,     233; R. A. Zelonka, M. C. Baird Can. J. Chem. 1972, 50, 3063 -   (ii) F. B. McCormick, D. D. Cox, W. B. Gleason Organomet. 1993, 12,     610 -   (iii) C. Solarzano, M. A. Davis Inorg. Chim. Acta 1985, 97, 135 -   M. G. B. Drew, C. M. Regan, S. M. Nelson J. Chem. Soc. Dalton trans.     1981, 1034 -   (v) R. G. Harvey Synthesis 1970, No. 4, 161 

1. A ruthenium (II) compound of formula (I):

wherein: R¹ is —CO₂CH₃; R², R³, R⁴, R⁵ and R⁶ independently represent H, alkyl, cycloalkyl, —CO₂R′, aryl or alkylaryl, which latter two groups are optionally substituted on the aromatic ring; R′ represents alkyl, cycloalkyl, aryl or alkaryl; X is halo, H₂O, (R′)(R″)SO, R′CO₂ ⁻ or (R′)(R″)C═O, where R″ represents alkyl, cycloalkyl, aryl or alkaryl; Y is a counterion; m is 0 or 1; q is 1, 2 or 3; C′ is C₁ to C₁₂ alkylene, optionally substituted in or on the alkylene chain, bound to two A groups; p is 0 or 1 and r is 1 when p is 0 and r is 2 when p is 1; and A and B are: each independently R¹¹—CN, where R¹¹ represents alkyl or; or B is halo and A is a 4-substituted pyridine; or p is 0, A is NR⁷R⁸ and B is NR⁹R¹⁰, wherein R⁷, R^(8,) R⁹ and R¹⁰ independently represent H, alkyl or cycloalkyl; and A and B are linked by an alkylene chain, optionally substituted in or on the alkylene chain; or p is 1, A is NR⁷ and B is NR⁹R¹⁰, wherein R⁷, R⁹ and R¹⁰ are as previously defined, and A and B are linked by an alkylene chain, optionally substituted.
 2. The compound as claimed in claim 1, wherein R², R³, R⁴, R⁵ and R⁶ all represent H.
 3. The compound as claimed in claim 1, wherein A and B are both R¹¹—CN and R¹¹ represents alkyl or cycloalkyl.
 4. The compound as claimed in claim 1, wherein A is a 4-substituted pyridine and B is halo.
 5. The compound as claimed in claim 1, wherein A and B together represent NR⁷R⁸—(CR¹²R¹³)_(m)—NR⁹R¹⁰, wherein R¹² and R¹³ are hydrogen, alkyl or cycloalkyl, and n is an integer from 1 to
 4. 6. The compound as claimed in claim 5, wherein R⁷, R⁸, R⁹ and R¹⁰ all represent H.
 7. The compound as claimed in claim 5, wherein R¹² and R¹³ are both H and n is
 2. 8. The compound as claimed in claim 5, wherein p is
 0. 9. The compound as claimed in claim 5, wherein R⁸ is absent, p is 1 and C′ is C₄ to C₁₀ straight chain alkylene.
 10. A ruthenium (II) compound of formula (I):

wherein: R¹ is phenyl; R², R³, R⁴, R⁵ and R⁶ independently represent H, alkyl, cycloalkyl, —CO₂R′, aryl or alkylaryl, which latter two groups are optionally substituted on the aromatic ring; R′ represents alkyl, cycloalkyl, aryl or alkaryl; X is halo, H₂O, (R′)(R″)SO, R′CO₂ ⁻ or (R′)(R″)C═O, where R″ represents alkyl, cycloalkyl, aryl or alkaryl; Y is a counterion; m is 0 or 1; q is 1, 2 or 3; C′ is C₁ to C₁₂ alkylene, optionally substituted in or on the alkylene chain, bound to two A groups; p is 0or 1 and r is 1 when p is 0 and r is 2 when p is 1; and A and B are: each independently R¹¹—CN where R¹¹ represents alkyl or cycloalkyl; or B is halo and A is a 4-substitued pyridine; or p is 0, A is NR⁷R⁸ and B is NR⁹R¹⁰, wherein R⁷, R⁸, R⁹ and R¹⁰ independently represent H, alkyl or cycloalkyl, and A and B are linked by an alkylene chain, optionally substituted in or on the alkylene chain; or p is 1, A is NR⁷ and B is NR⁹R¹⁰, wherein R⁷, R⁹ and R¹⁰ are as previously defined, and A and B are linked by an alkylene chain, optionally substituted.
 11. The compound as claimed in claim 10, wherein R², R³, R⁴, R⁵ and R⁶ all represent H.
 12. The compound as claimed in claim 10, wherein A and B are both R¹¹—CN and R¹¹ represents alkyl or cycloalkyl.
 13. The compound as claimed in claim 10, wherein A is a 4-substituted pyridine and B is halo.
 14. The compound as claimed in claim 10, wherein A and B together represent NR⁷R⁸—(CR¹²R¹³)_(m)NR⁹R¹⁰, wherein R¹² and R¹³ are hydrogen, alkyl or cycloalkyl, and n is an integer from 1 to
 4. 15. The compound as claimed in claim 14, wherein R⁷, R⁸, R⁹ and R¹⁰ all represent H.
 16. The compound as claimed in claim 14, wherein R¹² and R¹³ are both H and n is
 2. 17. The compound as claimed in claim 14, wherein p is
 0. 18. The compound as claimed in claim 14, wherein R⁸ is absent, p is 1 and C′ is C₄ to C₁₀ straight chain alkylene.
 19. A pharmaceutical composition comprising: (a) a ruthenium (II) compound of formula (I):

wherein: R¹, R², R³, R⁴, R⁵ and R⁶ independently represent H, alkyl, —CO₂R′, aryl, cycloalkyl, or alkylaryl, which latter two groups are optionally substituted on the aromatic ring; R′ represents alkyl, cycloalkyl, aryl or alkaryl; X is halo, H₂O, (R′)(R″)SO, R′CO₂ ⁻ or (R′)(R″)C═O, where R″ represents alkyl, cycloalkyl, aryl or alkaryl; Y is a counterion; m is 0 or 1; q is 1, 2 or 3; C′ is C₁ to C₁₂ alkylene, optionally substituted in or on the alkylene chain, bound to two A groups; p is 0 or 1 and r is 1 when p is 0 and r is 2 when p is 1; and A and B are: each independently R¹¹ —CN where R¹¹ represents alkyl or cycloalkyl; or B is halo and A is a 4-substitued pyridine; and (b) at least one pharmaceutically acceptable excipient.
 20. The composition as claimed in claim 19, wherein R², R³, R⁴, R⁵ and R⁶ all represent H.
 21. The composition as claimed in claim 19, wherein R¹ is H.
 22. The composition as claimed in claim 19, wherein R¹ is 2-propyl and R⁴ is methyl.
 23. The composition as claimed in claim 19, wherein R¹ is phenyl.
 24. The composition as claimed in claim 19, wherein R¹ is —CO₂CH₃.
 25. The composition as claimed in claim 19, wherein A and B are both R¹¹—CN and R¹¹ represents alkyl or cycloalkyl.
 26. The composition as claimed in claim 19, wherein A is a 4-substituted pyridine and B is halo.
 27. A method for treating ovarian cancer, comprising administering to a subject a therapeutically effective amount of a compound of formula (I):

wherein: R¹, R², R³, R⁴, R⁵ and R⁶ independently represent H, alkyl, cycloalkyl, —CO₂R′, aryl or alkylaryl, which latter two groups are optionally substituted on the aromatic ring; R′ represents alkyl, cycloalkyl, aryl or alkaryl; X is halo, H₂O, (R′)(R″)SO, R′CO₂ ⁻ or (R′)(R″)C═O, where R″ represents alkyl, cycloalkyl, aryl or alkaryl; Y is a counterion; m is 0 or 1; q is 1, 2 or 3; C′ is C₁ to C₁₂ alkylene, optionally substituted in or on the alkylene chain, bound to two A groups; p is 0 or 1 and r is 1 when p is 0 and r is 2 when p is 1; and A and B are: each independently R¹¹—CN where R¹¹ represents alkyl or cycloalkyl; or B is halo and A is a 4-substituted pyridine.
 28. The method as claimed in claim 27, wherein R², R³, R⁴, R⁵ and R⁶ all represent H.
 29. The method as claimed in claim 27, wherein R¹ is H.
 30. The method as claimed in claim 27, wherein R¹ is 2-propyl and R⁴ is methyl.
 31. The method as claimed in claim 27, wherein R¹ is phenyl.
 32. The method as claimed in claim 27, wherein R¹ is —CO₂CH₃.
 33. The method as claimed in claim 27, wherein A and B are both R¹¹—CN and R¹¹ represents alkyl or cycloalkyl.
 34. The method as claimed in claim 27, wherein A is a 4-substituted pyridine and B is halo. 